Arrowg+ard Blue Advance Midline Recalled for Incorrect Expiration Date
Arrow International Inc is recalling Arrowg+ard Blue Advance Midline devices due to an incorrect expiration date printed on the product.
The agency’s classification
FDA (Devices): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 2/5 (Moderate).
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II, and the hazard is a labeling error (incorrect expiration date) without reported injuries or illnesses, fitting the criteria for a moderate severity voluntary precautionary recall.
Plain-English summary
Arrow International Inc is recalling 430 units of Arrowg+ard Blue Advance Midline devices, Product Code PR 41541 BAS. The recall is being conducted because the product bears an incorrect expiration date.
The affected devices were distributed nationwide and to foreign markets. The specific batch code for the recalled units is 13F17L0170.
Consumers and healthcare providers should check their inventory for this specific product code and batch code. If the product is found, it should be removed from use and returned to the distributor or manufacturer according to their instructions.
The recalled product
- Product
- Arrowg+ard Blue Advance Midline Product Code: PR 41541 BAS
- Manufacturer
- Arrow International Inc
- Category
- Medical Device — IV Catheters
- Hazard
- Affected units
- 430
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- Batch Code:13F17L0170
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 36 recalled by Arrow International Inc under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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